Canonical Allele Identifier: CA353688950
Gene: GBE1 HGNC NCBI

Linked Data

dbSNP Id: rs1441953389
gnomAD v4: 3-81670902-C-T
MyVariant Identifiers: chr3:g.81720053C>T (hg19) chr3:g.81670902C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81670902C>T , CM000665.2:g.81670902C>T GRCh38
NC_000003.11:g.81720053C>T , CM000665.1:g.81720053C>T GRCh37
NC_000003.10:g.81802743C>T NCBI36
NG_011810.1:g.95899G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.365G>A MANE Select ENSP00000410833.2:p.Trp122Ter
ENST00000429644.6:c.365G>A ENSP00000410833.2:p.Trp122Ter
ENST00000477426.1:n.81G>A
ENST00000489715.1:c.242G>A ENSP00000419638.1:p.Trp81Ter
NM_000158.3:c.365G>A NP_000149.3:p.Trp122Ter
NM_000158.4:c.365G>A MANE Select NP_000149.4:p.Trp122Ter
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Search 100 bp 3'